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Home » Basic and Health Sciences » Chemistry » Advance Organic Chemistry (UCI) » 4.Stereochemistry Properties of Stereoisomers.(UCIRVINE)

4.Stereochemistry Properties of Stereoisomers.(UCIRVINE)

Course:Advance Organic Chemistry (UCI)
Discipline:Basic and Health Sciences
Institute:UCI Open
Instructor(s): Prof. Dr. James S. Nowick.
Level:Undergraduate

Advance Organic Chemistry (UCI)

1.Nomenclature Bicyclic Compounds. (UCIRVINE)
10. Linear Free-Energy Relationships.(UCIRVINE)
11. Molecular Orbitals and Aromaticity.(UCIRVINE)
12. Introduction to Pericyclic Reactions.(UCIRVINE)
13. Cycloadditions and Sigmatropic Rearrangements.(UCIRVINE)
14. Functional Group Transformation & Oxidation State.(UCIRVINE)
15. Oxidation & Reduction Alcohols & Carbonyl Compounds.(UCIRVINE)
16. Stereoselective Reduct.; Mitsunobu & Barton-Mc CombieRxns.(UCIRVINE)
17. The Carbonyl Group in Carbon-Carbon Bond Formation.(UCIRVINE)
18. Claisen Condensation and Michael Addition.(UCIRVINE)
19. Acid-Catalyzed Aldol Reactions and the Mannich Reaction.(UCIRVINE)
2.Spirocyclic, Polycyclic, & Heterocyclic Compounds.(UCIRVINE)
20. Enamines, the Wittig Reaction, and Cyclopropanation.(UCIRVINE)
21. Benzoin &Acyloin Condensations. Acyl Anion Equivalents.(UCIRVINE)
22. Retrosynthetic Analysis. Diels-Alder; Robinson Annulation.(UCIRVINE)
23. How Concentration, Stoichiometry, & Solvent Affect Rxns.(UCIRVINE)
24. How Temperature and Other Conditions Affect Reactions.(UCIRVINE)
25. NMR Spectroscopy How NMR Works. Chemical Shifts.(UCIRVINE)
26. Spin-Spin Coupling in 1H NMR Spectroscopy.(UCIRVINE)
27. Determining Stereochemistry and Regiochemistry by NMR.(UCIRVINE)

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